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Collembolispora aristata - Fungal Planet

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190 Persoonia – Volume 29, 2012<br />

<strong>Collembolispora</strong> <strong>aristata</strong>


<strong>Fungal</strong> <strong>Planet</strong> description sheets<br />

191<br />

<strong>Fungal</strong> <strong>Planet</strong> 149 – 20 December 2012<br />

<strong>Collembolispora</strong> <strong>aristata</strong> Marvanová & J.Z. Groenew., sp. nov.<br />

Etymology. aristatus (L.) = with bristles.<br />

Conidia isolated from foam according to the methodology of<br />

Marvanová et al. (2003). Colonies on malt agar medium fast<br />

growing, reaching 25 mm after 20 d at 12 °C, dark grey, reverse<br />

black. Aerial mycelium abundant, lanose to funiculose.<br />

Hyphae glabrous, hyaline, thin-walled, 1–3 µm wide or dark<br />

brown, thicker-walled, up to 5 µm wide. Sporulation initially<br />

directly on agar, in subcultures after submergence in standing<br />

distilled water at 15 °C within a few days. Conidiophores intercalary,<br />

lateral or terminal, simple to profusely branched; stipes,<br />

if present, cylindrical or distally slightly widening up to 32 ×<br />

1.5–3.5 µm, with branches on various levels along the stipes<br />

or in a penicillate head; often concurrent with conidiogenous<br />

cells, sometimes verticillate, cylindrical or subclavate, 4–8 ×<br />

2–3 µm. Conidiogenous cells subclavate to narrow-doliiform,<br />

usually 1–3 per conidiophore branch, polyblastic sympodial,<br />

5–11 × 1.5–3 µm, with one to few denticles at the apex, scars<br />

flat. Conidia in slimy masses when formed outside water, appearing<br />

in close sequence. Axis 31–46 × 2–3.5 µm, proximal<br />

part obclavate and unequilateral, mildly curved or straight,<br />

3(–5)-septate, basal scar truncate, sometimes eccentric,<br />

apex with an integrated, setose extension sometimes slightly<br />

curved away; branch single (exceptionally two), typically ventral,<br />

rarely dorsal, usually arising from the second suprabasal<br />

cell of the axis, often strongly retrorse, but also perpendicular<br />

to the axis, straight or often slightly curved abaxially, rarely<br />

adaxially, proximal part obclavate, base often slightly sinuous,<br />

16–30 × 1.5–2.7 µm, insertion unequally constricted, distally<br />

protracted into setose extension. Some considerably swollen<br />

conidia are usually present in submerged cultures after several<br />

weeks. Hyphopodia-like outgrowths may appear in aged,<br />

submerged cultures on hyphae, and also on conidia.<br />

Typus. Czech Republic, South Moravian region, between the villages<br />

Ochoz uTišnova and Lomnice, c. 440 m alt., isolated from foam in an unnamed<br />

left tributary of the Křeptovský potok stream (the streamlet is shallow,<br />

80–100 cm wide, slow-flowing, with grasses on the banks and Typha<br />

latifolia and Glyceria maxima in the littoral zone), Mar. 1984, L. Marvanová,<br />

holotype CBS H-21090, culture ex-type CPC 21145 = CCM F-01585 = CBS<br />

115662; ITS sequence GenBank KC005789, LSU sequence GenBank<br />

KC005811, MycoBank MB491201.<br />

Notes — The hyphomycete genus <strong>Collembolispora</strong> is<br />

based on C. barbata, isolated from Alnus glutinosa leaf baits<br />

submerged in a slow-flowing, oligotrophic softwater stream in<br />

North Portugal (Marvanová et al. 2003). <strong>Collembolispora</strong> <strong>aristata</strong><br />

has similar colonies, conidiogenesis as well as conidia<br />

like C. barbata, but the conidia of the latter differ from those of<br />

C. <strong>aristata</strong> by having a branched, terminal, setose extension<br />

on the conidial axis and on the conidial branch, and by the<br />

presence of a hyphomycetous, phialidic (?spermatial) morph.<br />

As far as we know, there is thus far only one other report on<br />

conidia of C. <strong>aristata</strong> (Roldán & Puig 1992, f. 3C, as Gyoerffyella<br />

sp.). These authors collected detached conidia in<br />

a stream in the river Esva basin in the Asturias Province of<br />

Northern Spain, 285 m alt., in a site where the riparian vegetation<br />

consists predominantly of grasses.<br />

Conidia of C. <strong>aristata</strong> resemble those of Ramulispora bromi,<br />

which is a grass parasite causing spots on Bromus spp. In fact<br />

the conidia illustrated by Sprague (1950, f. 76), resemble underdeveloped<br />

conidia of C. <strong>aristata</strong>, without long extensions.<br />

According to Braun (1995), R. bromi is an insufficiently known<br />

species, with conidia resembling those of Mycocentrospora<br />

or Spermospora. Ramulispora is based on R. andropogonis,<br />

which according to Braun (1995) is a facultative (taxonomic)<br />

synonym of R. sorghi, based on Septorella sorghi. Conidia of<br />

R. sorghi are filiform to narrow obclavate, sometimes with 1–2<br />

lateral branches. Ramulispora sorghi is anamorphic Mycosphaerellaceae,<br />

Dothideomycetes (Crous et al. 2009a, c).<br />

<strong>Collembolispora</strong> <strong>aristata</strong> conidia are superficially also similar<br />

to those of two Gyoerffyella species with single-branched<br />

non-coiled conidia (G. entomobryoides and G. tricapillata).<br />

However, members of this holoanamorphic genus have pale<br />

colonies and polyblastic, clavate conidiogenous cells, which<br />

do not proliferate.<br />

Phylogenetically <strong>Collembolispora</strong> clusters in the Helotiales,<br />

with the nearest group formed by strains of Leptodontidium<br />

orchidicola. Leptodontidium was established for dematiaceous<br />

endophytes in roots of various plants growing in cool<br />

soils rich in humus (Fernando & Currah 1995). Based on a<br />

megablast search of NCBIs GenBank nucleotide database,<br />

the closest hits using the LSU sequence are Cadophora luteoolivacea<br />

(GenBank HM116760; Identities = 907/913 (99 %),<br />

Gaps = 0/913 (0 %)) and Mollisia dextrinospora (GenBank<br />

HM116757; Identities = 906/913 (99 %), Gaps = 0/913 (0 %)).<br />

Closest hits using the ITS sequence had highest similarity to<br />

<strong>Collembolispora</strong> barbata (GenBank GQ411302; Identities =<br />

559/576 (97 %), Gaps = 7/576 (1 %)) and Leptodontidium orchidicola<br />

(GenBank GU586841; Identities = 555/580 (96 %),<br />

Gaps = 10/580 (2 %)).<br />

There is little information on the ecology of species of <strong>Collembolispora</strong>.<br />

It is not known whether they should be considered<br />

indwellers, residents or transients (in the sense of Park 1972)<br />

in the water environment. In both localities of C. <strong>aristata</strong>, Poaceae<br />

were present on the stream banks or in the littoral zone.<br />

Although the occurrence of Poaceae at the type locality may<br />

support the hypothesis about relationships between R. bromi<br />

and C. <strong>aristata</strong>, the phylogenetic affinity suggests this not to<br />

be the case.<br />

Colour illustrations. Left tributary of the stream Křeptovský potok between<br />

the villages Ochoz u Tišnova and Lomnice; conidiophores, conidiogenous<br />

cells and appendaged conidia. Scale bars = 10 µm.<br />

Ludmilla Marvanová, Czech Collection of Microorganisms, Institute of Experimental Biology, Faculty of Science, Masaryk University,<br />

Tvrdého 14, 602 00 Brno, Czech Republic; e-mail: ludmila@sci.muni.cz<br />

Johannes Z. Groenewald, CBS-KNAW <strong>Fungal</strong> Biodiversity Centre, P.O. Box 85167, 3508 AD Utrecht, The Netherlands;<br />

e-mail: e.groenewald@cbs.knaw.nl<br />

© 2012 Nationaal Herbarium Nederland & Centraalbureau voor Schimmelcultures

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